Evidence map›Paper›PMID 29660934›Full record

ArticleJournal of Alzheimer's disease : JAD2018

Bi-directional Association of Cerebrospinal Fluid Immune Markers with Stage of Alzheimer's Disease Pathogenesis.

Pierre-François Meyer, Melissa Savard, Judes Poirier, Anne Labonté, Pedro Rosa-Neto, Tara M Weitz, Terrence Town, John Breitner, Alzheimer’s Disease Neuroimaging Initiative, PREVENT-AD Research Group

Abstract read
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
  2. No apparent effect of naproxen on CSF markers of innate immune activation.Annals of clinical and translational neurology · 2019
    Trial
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Osteopontin: A novel marker of pre-symptomatic sporadic Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Charting the Next Road Map for CSF Biomarkers in Alzheimer's Disease and Related Dementias.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Knowledge gaps in Alzheimer's disease immune biomarker research.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2021
    Review
  19. Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 2 countries.

Pierre-François MeyerFaculty of Medicine, McGill University, Montréal, QC, Canada.
Melissa SavardCenter for Studies on the Prevention of Alzheimer's Disease (StoP-AD), Douglas Mental Health University Institute, Montréal, QC, Canada.
Judes PoirierFaculty of Medicine, McGill University, Montréal, QC, Canada.
Anne LabontéCenter for Studies on the Prevention of Alzheimer's Disease (StoP-AD), Douglas Mental Health University Institute, Montréal, QC, Canada.
Pedro Rosa-NetoFaculty of Medicine, McGill University, Montréal, QC, Canada.
Tara M WeitzZilkha Neurogenetic Institute, Keck School of Medicine of the University of Southern California, Los Angeles, CA, USA.
Terrence TownZilkha Neurogenetic Institute, Keck School of Medicine of the University of Southern California, Los Angeles, CA, USA.
John BreitnerFaculty of Medicine, McGill University, Montréal, QC, Canada.
Alzheimer’s Disease Neuroimaging Initiative
PREVENT-AD Research Group
Douglas Mental Health University Institute · CAUniversity of Southern California · US

Funding

Alzheimer's Disease Neuroimaging Initiative - SupplementU01AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI WEINER, MICHAEL W · 2004 to 2015
$121.0M
Peripheral TGF-beta Pathway Inhibitor Therapy in Alzheimer's RatsR01NS076794 · NINDS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHANG, KAREN T, CHEN, JEANNIE · 2011 to 2021
$4.9M
Innate Immune IL-10/STAT3 Signaling in Alzheimer's DiseaseRF1AG053982 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHANG, KAREN T, CHEN, JEANNIE · 2017 to 2017
$2.8M
CIHRNIA NIH HHS R01 AG053982NIA NIH HHS RF1 AG053982NIA NIH HHS U01 AG024904NINDS NIH HHS R01 NS076794
6 · The paper itself

Abstract

Immune mechanisms may be important in the pathogenesis of Alzheimer's disease (AD). Yet, studies comparing cerebrospinal fluid (CSF) and plasma immune marker levels of healthy and demented individuals have yielded conflicting results. We analyzed CSF from 101 members of the parental history-positive PREVENT-AD cohort of healthy aging adults, and 237 participants without dementia from the initial cohort of the Alzheimer's Disease Neuroimaging Initiative (ADNI-1). Following recent practice, we used the biomarkers total-tau and amyloid-β1-42 to allocate participants from each study into four stages of AD pathogenesis: Stage 0 (no abnormality), Stage 1 (reduced amyloid-β1-42), Stage 2 (reduced amyloid-β1-42 and increased total-tau), or "Suspected Non-Alzheimer Pathology" (elevated total-tau only). Investigating the PREVENT-AD participants' CSF assay results for 19 immune/inflammatory markers, we found six that showed a distinct bi-directional relationship with pathogenetic stage. Relative to Stage 0, these were diminished at Stage 1 but strongly increased at Stage 2. Among the ADNI participants (90 healthy controls and 147 with mild cognitive impairment), we found that 23 of 83 available CSF markers also showed this distinct pattern. These results support recent observations that immune activation may become apparent only after the onset of both amyloid and tau pathologies. Unexpectedly, they also suggest that immune marker activity may diminish along with earliest appearance of amyloid-β plaque pathology. These findings may explain discordant results from past studies, and suggest the importance of characterizing the extent of AD pathology when comparing clinical groups.

Indexed as

AgedAlzheimer DiseaseAmyloid beta-PeptidesApolipoproteins EBiomarkersCohort StudiesFemaleHumansInflammationMaleMiddle AgedPeptide Fragmentstau ProteinsAmyloid beta-Peptidesamyloid beta-protein (1-42)Apolipoproteins EBiomarkersMAPT protein, humanPeptide Fragmentstau ProteinsAlzheimer’s diseasebiomarkersinflammationpathology

Identifiers

PMID29660934
PMCPMC5929310
OpenAlexW2796827135

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.